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Clinical Research Coordinator

Job in Orange, Orange County, California, 92613, USA
Listing for: SoTalent
Full Time position
Listed on 2026-01-17
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 60000 - 72000 USD Yearly USD 60000.00 72000.00 YEAR
Job Description & How to Apply Below

Location: Orange, CA

Estimated Salary: $60,000–$72,000 annually

Employment Type: Full-time, Onsite

The Opportunity

A leading healthcare and research organization is seeking a Clinical Research Coordinator to oversee the day-to-day operations of multiple clinical research studies. This role plays a critical part in ensuring study integrity, regulatory compliance, and seamless coordination between investigators, patients, sponsors, and regulatory bodies.

You’ll work closely with the Principal Investigator to ensure strict adherence to study protocols and Good Clinical Practice (GCP/ICH) standards, while maintaining accurate, timely documentation across all studies.

What You’ll Do
  • Coordinate and manage daily operations of multiple clinical research studies
  • Serve as the primary liaison between the Principal Investigator, patients, sponsors, and the Institutional Review Board (IRB)
  • Ensure all study documentation is accurate, complete, and submitted on time
  • Support compliance with study protocols, GCP/ICH guidelines, and regulatory requirements
  • Assist with patient coordination and study‑related procedures as required
  • Maintain organized research files and support audits and inspections
Key Responsibilities
  • Monitor study progress and ensure protocol adherence
  • Coordinate communication across internal and external research stakeholders
  • Maintain regulatory binders and study documentation
  • Support data integrity and quality control initiatives
  • Assist with biohazard material handling and sample logistics where applicable
What You Bring
  • Completion of an accredited Medical or Phlebotomy training program, or equivalent education/experience
  • 2+ years of experience in a clinical research setting (3 years preferred)
  • Working knowledge of clinical trial operations and regulatory standards
  • Strong organizational skills with exceptional attention to detail
  • Ability to manage multiple studies simultaneously in a fast‑paced environment
  • Clear, professional communication skills
Preferred Qualifications
  • College degree or vocational school graduate
  • Biohazardous materials packaging training
  • Experience working in hospital‑ or clinic‑based clinical research environments
Why This Role

This position offers the opportunity to contribute to meaningful clinical research within a patient‑centered healthcare environment
, while gaining exposure to complex studies, multidisciplinary teams, and long‑term career growth in clinical research.

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